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Results: 4

Authors: Boycott, KM Maybaum, TA Naylor, MJ Weleber, RG Robitaille, J Miyake, Y Bergen, AAB Pierpont, ME Pearce, WG Bech-Hansen, NT
Citation: Km. Boycott et al., A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants, HUM GENET, 108(2), 2001, pp. 91-97

Authors: Ells, A Harvey, P Hindle, W LaRoche, GR Little, J Lyons, C Robitaille, J Shuckett, P Vincer, M White, J
Citation: A. Ells et al., Guidelines for screening examinations for retinopathy of prematurity, CAN J OPHTH, 35(5), 2000, pp. 251-252

Authors: Koenekoop, R Pina, AL Loyer, M Davidson, J Robitaille, J Maumenee, I Tombran-Tink, J
Citation: R. Koenekoop et al., Four polymorphic variations in the PEDF gene identified during the mutation screening of patients with Leber congenital amaurosis, MOL VIS, 5(10), 1999, pp. NIL_1-NIL_4

Authors: Robitaille, J Izzi, L Daniels, E Zelus, B Holmes, KV Beauchemin, N
Citation: J. Robitaille et al., Comparison of expression patterns and cell adhesion properties of the mouse biliary glycoproteins Bgp1 and Bgp2, EUR J BIOCH, 264(2), 1999, pp. 534-544
Risultati: 1-4 |